Page last updated: 2024-10-28

miltefosine and Trypanosomiasis

miltefosine has been researched along with Trypanosomiasis in 4 studies

miltefosine: hexadecyl phosphocholine derivative of cisplatin; did not substantially activate HIV long terminal repeat; less toxic than cisplatin
miltefosine : A phospholipid that is the hexadecyl monoester of phosphocholine.

Trypanosomiasis: Infection with protozoa of the genus TRYPANOSOMA.

Research Excerpts

ExcerptRelevanceReference
" In this study, a new semi-synthetic berberine analogue, 5,6-didehydro-8,8-diethyl-13-oxodihydroberberine chloride (1), showed nanomolar level potency against in vitro models of leishmaniasis, malaria, and trypanosomiasis as well as activity in an in vivo visceral leishmaniasis model."3.77Potent antiprotozoal activity of a novel semi-synthetic berberine derivative. ( Anklin, C; Bahar, M; Deng, Y; Doskotch, RW; Drew, ME; Gil, RR; He, S; Kinghorn, AD; Navarro-Vázquez, A; Pandharkar, T; Werbovetz, KA; Zhu, X, 2011)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Holloway, GA1
Charman, WN1
Fairlamb, AH1
Brun, R1
Kaiser, M1
Kostewicz, E1
Novello, PM1
Parisot, JP1
Richardson, J1
Street, IP1
Watson, KG1
Baell, JB1
Bahar, M1
Deng, Y1
Zhu, X1
He, S1
Pandharkar, T1
Drew, ME1
Navarro-Vázquez, A1
Anklin, C1
Gil, RR1
Doskotch, RW1
Werbovetz, KA1
Kinghorn, AD1
Bosc, D1
Mouray, E1
Cojean, S1
Franco, CH1
Loiseau, PM1
Freitas-Junior, LH1
Moraes, CB2
Grellier, P1
Dubois, J1
Linciano, P1
Pozzi, C1
Iacono, LD1
di Pisa, F1
Landi, G1
Bonucci, A1
Gul, S1
Kuzikov, M1
Ellinger, B1
Witt, G1
Santarem, N1
Baptista, C1
Franco, C1
Müller, W1
Wittig, U1
Luciani, R1
Sesenna, A1
Quotadamo, A1
Ferrari, S1
Pöhner, I1
Cordeiro-da-Silva, A1
Mangani, S1
Costantino, L1
Costi, MP1

Other Studies

4 other studies available for miltefosine and Trypanosomiasis

ArticleYear
Trypanothione reductase high-throughput screening campaign identifies novel classes of inhibitors with antiparasitic activity.
    Antimicrobial agents and chemotherapy, 2009, Volume: 53, Issue:7

    Topics: Animals; Antiparasitic Agents; Drug Evaluation, Preclinical; Humans; Microsomes, Liver; Molecular St

2009
Potent antiprotozoal activity of a novel semi-synthetic berberine derivative.
    Bioorganic & medicinal chemistry letters, 2011, May-01, Volume: 21, Issue:9

    Topics: Animals; Antiprotozoal Agents; Berberine; Chlorocebus aethiops; Disease Models, Animal; Inhibitory C

2011
Highly improved antiparasitic activity after introduction of an N-benzylimidazole moiety on protein farnesyltransferase inhibitors.
    European journal of medicinal chemistry, 2016, Feb-15, Volume: 109

    Topics: Alkyl and Aryl Transferases; Animals; Antiparasitic Agents; Cell Line; Enzyme Inhibitors; Humans; Im

2016
Enhancement of Benzothiazoles as Pteridine Reductase-1 Inhibitors for the Treatment of Trypanosomatidic Infections.
    Journal of medicinal chemistry, 2019, 04-25, Volume: 62, Issue:8

    Topics: Animals; Antiprotozoal Agents; Benzothiazoles; Binding Sites; Catalytic Domain; Crystallography, X-R

2019